» Articles » PMID: 4005141

Chemosensitivity Measurements of Human Tumour Cells by Soft Agar Assays Are Influenced by the Culture Conditions

Overview
Journal Br J Cancer
Specialty Oncology
Date 1985 Jun 1
PMID 4005141
Citations 6
Authors
Affiliations
Soon will be listed here.
Abstract

To investigate the influence of culture conditions on the in vitro responses of tumour cells to anticancer drugs, the sensitivities observed with the soft agar methods of Hamburger & Salmon (1977) (H-S) and of Courtenay & Mills (1978) (C-M) were compared. In all cases the ID50 values were determined from dose-response curves. Six human tumour cell lines exposed to 10 different agents, and 9 patients' melanomas exposed to 5 different agents, were examined. In the studies of cell lines the H-S method gave higher sensitivity values than the C-M method in 38 out of 52 cases, whereas in 14 cases the results were the same. In the patients' tumours the H-S method gave higher sensitivity in 21 of 35 cases, equal sensitivity in 11, and lower sensitivity in 3 cases. In many instances the ID50 values obtained with the two test systems differed by factors of 10 or more, both in the case of cell lines and tumour specimens. Systematic alterations in the culture conditions indicated that the presence or absence of rat erythrocytes is the most important factor responsible for the differences observed. Also, other factors, such as supplements (in the H-S method) and the use of different serum types, appeared to influence both colony growth and chemosensitivity.

Citing Articles

Pre-clinical evaluation of tyrosine kinase inhibitors for treatment of acute leukemia.

Christoph S, Lee-Sherick A, Sather S, DeRyckere D, Graham D J Vis Exp. 2013; (79):e50720.

PMID: 24084362 PMC: 3923888. DOI: 10.3791/50720.


Effects of 4-hydroxytamoxifen and a novel pure antioestrogen (ICI 182780) on the clonogenic growth of human breast cancer cells in vitro.

DeFriend D, Anderson E, Bell J, Wilks D, West C, Mansel R Br J Cancer. 1994; 70(2):204-11.

PMID: 8054267 PMC: 2033516. DOI: 10.1038/bjc.1994.281.


Selection of tumour cell subpopulations occurs during cultivation of human tumours in soft agar. A DNA flow cytometric study.

Tveit K, Pettersen E, Fossa S, Pihl A Br J Cancer. 1985; 52(5):701-5.

PMID: 4063145 PMC: 1977230. DOI: 10.1038/bjc.1985.246.


Multicellular spheroids. A review on cellular aggregates in cancer research.

Mueller-Klieser W J Cancer Res Clin Oncol. 1987; 113(2):101-22.

PMID: 3549738 DOI: 10.1007/BF00391431.


Radiation survival of murine and human melanoma cells utilizing two assay systems: monolayer and soft agar.

Yohem K, Slymen D, Bregman M, Meyskens Jr F Br J Cancer. 1988; 57(1):64-9.

PMID: 3348949 PMC: 2246683. DOI: 10.1038/bjc.1988.10.


References
1.
Hill B, Whelan R . Attempts to optimise colony-forming efficiencies using three different survival assays and a range of human tumour continuous cell lines. Cell Biol Int Rep. 1983; 7(8):617-24. DOI: 10.1016/0309-1651(83)90116-9. View

2.
Joyce R, Vincent P . Advantage of reduced oxygen tension in growth of human melanomas in semi-solid cultures: quantitative analysis. Br J Cancer. 1983; 48(3):385-93. PMC: 2011479. DOI: 10.1038/bjc.1983.203. View

3.
Hamburger A, Salmon S . Primary bioassay of human tumor stem cells. Science. 1977; 197(4302):461-3. DOI: 10.1126/science.560061. View

4.
COURTENAY V, Mills J . An in vitro colony assay for human tumours grown in immune-suppressed mice and treated in vivo with cytotoxic agents. Br J Cancer. 1978; 37(2):261-8. PMC: 2009601. DOI: 10.1038/bjc.1978.35. View

5.
Tveit K, Fodstad O, JOHANNESSEN J, Olsnes S . A human melanoma cell line established from xenograft in athymic mice. Br J Cancer. 1980; 41(5):724-33. PMC: 2010317. DOI: 10.1038/bjc.1980.134. View